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N/A N=252 Randomized Health Services Research

Antimicrobial Stewardship Through MRSA Diagnosis in Emergency Department (ED) Patients With Abscesses

Cutaneous Abscess

Enrolled (actual)
252
Serious AEs
Results posted
Sep 2017
Primary outcome: Primary: Number of Participants With Antibiotic Usage at the Time of the ED Visit — 97; 96 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Xpert MRSA/SA SSTI (Device); Standard culture (Diagnostic_test)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
George Washington University
Primary completion
Jan 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Antibiotic Usage at the Time of the ED Visit
97; 96
SECONDARY
Participant Clinical Improvement Post-treatment at One Week
91; 94 >0.05
SECONDARY
Clinical Outcome at One or Three Months
26; 24

Summary

This study expands upon pilot data for feasibility since May 2011. The study aims to evaluate the effect of rapid test availability on use of targeted spectrum antibiotics for non-MRSA abscesses in ambulatory patients in the Emergency Department (ED). The multi-institutional study will assess the feasibility of providing the GeneXpert® MRSA/SA SSTI assay to the ED and evaluate the impact of delivering the test result to clinicians in real-time on patient management decisions regarding the use of antimicrobial agents. Patients are randomized to standard culture (control arm) or to the GeneXpert® assay plus standard culture.

Eligibility Criteria

Inclusion Criteria

  • adults 18 years or older with community onset abscess

Exclusion Criteria

  • previous treatment for same abscess in past 14 days
  • postoperative infection
  • inability to provide informed consent
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01523899). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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